A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024551



Internal ID19113768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109901687..110003957hg38UCSC Ensembl
Innerchr7:109541744..109644014hg19UCSC Ensembl
Innerchr7:109328980..109431250hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38102271
hg19102271
hg18102271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645203, nssv3645204
Samples
Known GenesEIF3IP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024551
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer